Canonical Allele Identifier: CA1200471904

Gene: LMNA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156134826C= , CM000663.2:g.156134826C=	GRCh38
NC_000001.10:g.156104617C= , CM000663.1:g.156104617C=	GRCh37
NC_000001.9:g.154371241C=	NCBI36
NG_008692.2:g.57254C= , LRG_254:g.57254C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.103C=	ENSP00000426535.3:p.Arg35=
ENST00000682650.1:c.661C=	ENSP00000506904.1:p.Arg221=
ENST00000683032.1:c.661C=	ENSP00000506771.1:p.Arg221=
ENST00000684195.1:c.661C=	ENSP00000508220.1:p.Arg221=
ENST00000361308.9:c.661C=	ENSP00000355292.6:p.Arg221=
ENST00000368300.9:c.661C= MANE Select	ENSP00000357283.4:p.Arg221=
ENST00000496738.6:n.1036C=
ENST00000504687.6:c.-4C=	ENSP00000426535.2:n.-4C=
ENST00000674518.1:c.*11C=	ENSP00000502261.1:n.*11C=
ENST00000674600.1:c.*460C=	ENSP00000501666.1:n.*460C=
ENST00000674720.1:c.661C=	ENSP00000502798.1:p.Arg221=
ENST00000675431.1:n.354C=
ENST00000675455.1:c.*461C=	ENSP00000501795.1:n.*461C=
ENST00000675667.1:c.661C=	ENSP00000501803.1:p.Arg221=
ENST00000675874.1:c.*132C=	ENSP00000501851.1:n.*132C=
ENST00000675881.1:c.661C=	ENSP00000501670.1:p.Arg221=
ENST00000675939.1:c.661C=	ENSP00000502256.1:p.Arg221=
ENST00000675989.1:n.1036C=
ENST00000676208.1:c.661C=	ENSP00000502468.1:p.Arg221=
ENST00000676283.1:n.1036C=
ENST00000676385.2:c.661C=	ENSP00000502091.1:p.Arg221=
ENST00000676434.1:c.661C=	ENSP00000501648.1:p.Arg221=
ENST00000677389.1:c.661C= MANE Plus Clinical	ENSP00000503633.1:p.Arg221=
ENST00000347559.6:c.661C=	ENSP00000292304.3:p.Arg221=
ENST00000361308.8:c.661C=	ENSP00000355292.5:p.Arg221=
ENST00000368297.5:c.418C=	ENSP00000357280.1:p.Arg140=
ENST00000368299.7:c.661C=	ENSP00000357282.3:p.Arg221=
ENST00000368300.8:c.661C=	ENSP00000357283.4:p.Arg221=
ENST00000368301.6:c.661C=	ENSP00000357284.2:p.Arg221=
ENST00000448611.6:c.325C=	ENSP00000395597.2:p.Arg109=
ENST00000473598.6:c.364C=	ENSP00000421821.1:p.Arg122=
ENST00000496738.5:n.6C=
ENST00000504687.5:c.412C=	ENSP00000426535.1:p.Arg138=
ENST00000515459.5:c.*335C=	ENSP00000424518.1:n.*335C=
ENST00000515824.1:n.22C=
NM_001257374.2:c.325C=	NP_001244303.1:p.Arg109=
NM_001282624.1:c.418C=	NP_001269553.1:p.Arg140=
NM_001282625.1:c.661C=	NP_001269554.1:p.Arg221=
NM_001282626.1:c.661C=	NP_001269555.1:p.Arg221=
NM_005572.3:c.661C= , LRG_254t1:c.661C=	NP_005563.1:p.Arg221=
NM_170707.3:c.661C=	NP_733821.1:p.Arg221=
NM_170708.3:c.661C=	NP_733822.1:p.Arg221=
XM_011509533.1:c.325C=	XP_011507835.1:p.Arg109=
XM_011509534.1:c.-4C=	XP_011507836.1:n.-4C=
XR_921781.1:n.910C=
XM_011509534.2:c.-4C=	XP_011507836.1:n.-4C=
XR_921781.2:n.908C=
NM_170707.4:c.661C= MANE Select	NP_733821.1:p.Arg221=
NM_001257374.3:c.325C=	NP_001244303.1:p.Arg109=
NM_001282626.2:c.661C=	NP_001269555.1:p.Arg221=
NM_001282624.2:c.418C=	NP_001269553.1:p.Arg140=
NM_001282625.2:c.661C=	NP_001269554.1:p.Arg221=
NM_005572.4:c.661C= MANE Plus Clinical	NP_005563.1:p.Arg221=
NM_170708.4:c.661C=	NP_733822.1:p.Arg221=